(9H-Fluoren-9-yl)methyl tert-butyl ethane-1,2-diyldicarbamate
97%
- Product Code: 37154
CAS:
166410-28-2
Molecular Weight: | 382.4529 g./mol | Molecular Formula: | C₂₂H₂₆N₂O₄ |
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Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amines. Its fluorenylmethyl (Fmoc) group is widely employed in solid-phase peptide synthesis (SPPS) to temporarily shield amino groups during the assembly of peptide chains. The tert-butyl group further enhances stability, making it resistant to acidic conditions, while allowing selective deprotection under mild basic conditions. This selectivity is crucial for constructing complex peptides without unwanted side reactions. Additionally, its application extends to the synthesis of other bioactive molecules, where precise control over functional groups is essential. Its stability and ease of removal make it a valuable tool in pharmaceutical research and development.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿6,174.00 |
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(9H-Fluoren-9-yl)methyl tert-butyl ethane-1,2-diyldicarbamate
This chemical is primarily used in organic synthesis, particularly in peptide chemistry, where it serves as a protecting group for amines. Its fluorenylmethyl (Fmoc) group is widely employed in solid-phase peptide synthesis (SPPS) to temporarily shield amino groups during the assembly of peptide chains. The tert-butyl group further enhances stability, making it resistant to acidic conditions, while allowing selective deprotection under mild basic conditions. This selectivity is crucial for constructing complex peptides without unwanted side reactions. Additionally, its application extends to the synthesis of other bioactive molecules, where precise control over functional groups is essential. Its stability and ease of removal make it a valuable tool in pharmaceutical research and development.
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